Skip to main content

Naphthylhydroxylamine

ADVERTISEMENT
Identification
Molecular formula
C10H9NO
CAS number
830-03-5
IUPAC name
N-(1-naphthyl)hydroxylamine
State
State

At room temperature, Naphthylhydroxylamine is found in a solid state. It is typically handled as a crystalline powder in laboratory settings.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.00
Boiling point (Celsius)
135.00
Boiling point (Kelvin)
408.00
General information
Molecular weight
159.19g/mol
Molar mass
159.1920g/mol
Density
1.2000g/cm3
Appearence

Naphthylhydroxylamine typically appears as a white crystalline solid. Its crystalline nature is indicative of its purity and it is generally used in its solid form for various chemical applications.

Comment on solubility

Solubility of N-(1-naphthyl)hydroxylamine

N-(1-naphthyl)hydroxylamine, a compound with a significant chemical structure, exhibits notable solubility characteristics. Understanding its solubility profile is essential for its application in various chemical processes and reactions.

Typically, the solubility of this compound can be summarized as follows:

  • Solvent Compatibility: N-(1-naphthyl)hydroxylamine is known to be soluble in polar organic solvents such as ethanol and methanol, enabling its use in various chemical syntheses.
  • Water Solubility: While it can demonstrate limited solubility in water, the presence of the hydroxylamine group contributes to its moderate interaction with this solvent.
  • Temperature Effects: Increasing temperature often enhances its solubility in organic solvents, as solvation dynamics can improve at elevated temperatures.
  • Concentration Dependency: The solubility tends to decrease significantly at higher concentrations, which can lead to precipitation in saturated solutions.

Overall, understanding the solubility of N-(1-naphthyl)hydroxylamine is crucial for effectively leveraging its chemical properties in practical applications. As always, it is important to consider the specific conditions in which this compound is used, as solvent choice and environmental factors can greatly influence solubility outcomes.

Interesting facts

Interesting Facts about N-(1-naphthyl)hydroxylamine

N-(1-naphthyl)hydroxylamine is an intriguing organic compound primarily used in chemical synthesis and analysis. Here are some fascinating aspects of this compound that highlight its significance in the field of chemistry:

  • Functional Group: This compound features a hydroxylamine functional group, which is known for its ability to form stable oximes with carbonyl compounds, making it a valuable reagent in organic synthesis.
  • Applications in Research: N-(1-naphthyl)hydroxylamine is often utilized in the investigation of nitroso compounds and can be employed in creating azo dyes, showcasing its versatility in organic chemistry.
  • Role in Chemical Reactions: It acts as a reducing agent in various chemical reactions, contributing to the formation of intermediates that are crucial in synthetic pathways.
  • Biological Relevance: There has been research indicating that derivatives of hydroxylamines, including this compound, may possess antioxidative properties, providing insight into potential therapeutic applications.

Moreover, the 1-naphthyl moiety in this compound lends it unique electronic characteristics. These properties can enhance reactivity and selectivity in chemical reactions:

  • Electron Density: The naphthyl group increases electron density, influencing reaction pathways.
  • Stabilization of Intermediates: The compound can stabilize certain reactive intermediates, making it a useful tool for chemists in synthesizing complex molecules.

As noted by chemists, "The versatility of N-(1-naphthyl)hydroxylamine in synthetic routes and its role as a reagent in analytical chemistry cannot be overstated." This compound serves as a bridge between theoretical research and practical applications in materials science and organic chemistry.

Synonyms
1-NAPHTHYLHYDROXYLAMINE
N-Hydroxy-1-naphthylamine
N-Hydroxy-1-naphthalenamine
N-Hydroxy-1-aminonaphthalene
N-hydroxynaphthalen-1-amine
CCRIS 1175
HSDB 2142
BRN 2638939
UNII-5O045G232P
CHEBI:34871
DTXSID40209510
4-15-00-00026 (Beilstein Handbook Reference)
HYDROXY-1-NAPHTHALENAMINE, N-
1-NAPHTHYLHYDROXYLAMINE [HSDB]
N-(1-Naphthyl)hydroxylamine
1Naphthylhydroxylamine
NHydroxy1naphthylamine
N1Naphthylhydroxylamine
1Hydroxyaminonaphthalene
NHydroxy1naphthalenamine
alphaNaphthylhydroxylamine
NHydroxy1aminonaphthalene
Hydroxylamine, N1naphthyl
1Naphthalenamine, Nhydroxy
DTXCID90132001
1-Hydroxyaminonaphthalene
607-30-7
alpha-Naphthylhydroxylamine
N-1-Naphthylhydroxylamine
N-naphthalen-1-ylhydroxylamine
N-(naphthalen-1-yl)hydroxylamine
Hydroxylamine, N-1-naphthyl-
1-Naphthalenamine, N-hydroxy-
5O045G232P
a-naphthylhydroxylamine
1-Naphthylhydroxylamin
CHEMBL261899
SCHEMBL2166547
AKOS006280162
Q26840867